Vanilloid receptor ligands and their use in treatments

ABSTRACT

Substituted nitrogen-containing heterocycles and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.

This application claims the benefit of U.S. Provisional Application No. 60/621,139 filed Oct. 22, 2004, which is hereby incorporated by reference.

BACKGROUND

The vanilloid receptor 1 (VR1) is the molecular target of capsaicin, the active ingredient in hot peppers. Julius et al. reported the molecular cloning of VR1 (Caterina et al., 1997). VR1 is a non-selective cation channel which is activated or sensitized by a series of different stimuli including capsaicin and resiniferatoxin (exogenous activators), heat & acid stimulation and products of lipid bilayer metabolism, anandamide (Premkumar et al., 2000, Szabo et al., 2000, Gauldie et al., 2001, Olah et al., 2001) and lipoxygenase metabolites (Hwang et al., 2000). VR1 is highly expressed in primary sensory neurons (Caterina et al., 1997) in rats, mice and humans (Onozawa et al., 2000, Mezey et al., 2000, Helliwell et al., 1998, Cortright et al., 2001). These sensory neurons innervate many visceral organs including the dermis, bones, bladder, gastrointestinal tract and lungs; VR1 is also expressed in other neuronal and non-neuronal tissues including but not limited to, CNS nuclei, kidney, stomach and T-cells (Nozawa et al., 2001, Yiangou et al., 2001, Birder et al., 2001). Presumably expression in these various cells and organs may contribute to their basic properties such as cellular signaling and cell division.

Prior to the molecular cloning of VR1, experimentation with capsaicin indicated the presence of a capsaicin sensitive receptor, which could increase the activity of sensory neurons in humans, rats and mice (Holzer, 1991; Dray, 1992, Szallasi and Blumberg 1996, 1999). The results of acute activation by capsaicin in humans was pain at injection site and in other species increased behavioral sensitivity to sensory stimuli (Szallasi and Blumberg, 1999). Capsaicin application to the skin in humans causes a painful reaction characterized not only by the perception of heat and pain at the site of administration but also by a wider area of hyperalgesia and allodynia, two characteristic symptoms of the human condition of neuropathic pain (Holzer, 1991). Taken together, it seems likely that increased activity of VR1 plays a significant role in the establishment and maintenance of pain conditions. Topical or intradermal injection of capsaicin has also been shown to produce localized vasodilation and edema production (Szallasi and Blumberg 1999, Singh et al., 2001). This evidence indicates that capsaicin through it's activation of VR1 can regulate afferent and efferent function of sensory nerves. Sensory nerve involvement in diseases could therefore be modified by molecules which effect the function of the vanilloid receptor to increase or decrease the activity of sensory nerves.

VR1 gene knockout mice have been shown to have reduced sensory sensitivity to thermal and acid stimuli (Caterina et al., 2000)). This supports the concept that VR1 contributes not only to generation of pain responses (i.e. via thermal, acid or capsaicin stimuli) but also to the maintenance of basal activity of sensory nerves. This evidence agrees with studies demonstrating capsaicin sensitive nerve involvement in disease. Primary sensory nerves in humans and other species can be made inactive by continued capsaicin stimulation. This paradigm causes receptor activation induced desensitization of the primary sensory nerve—such reduction in sensory nerve activity in vivo makes subjects less sensitive to subsequent painful stimuli. In this regard both capsaicin and resinferatoxin (exogenous activators of VR1), produce desensitization and they have been used for many proof of concept studies in in vivo models of disease (Holzer, 1991, Dray 1992, Szallasi and Blumberg 1999).

BIBLIOGRAPHY

-   Birder-L A. Kanai-A J. de-Groat-W C. Kiss-S. Nealen-M L. Burke-N E.     Dineley-K E. Watkins-S. Reynolds-I J. Caterina-M J. (2001) Vanilloid     receptor expression suggests a sensory role for urinary bladder     epithelial cells. PNAS 98: 23: 13396-13401. -   Caterina, M. J, Schumacher, M. A., Tominaga, M., Rosen, T. A.,     Levine, J. D., and Julius, D, (1997). The capsaicin receptor: a     heat-activated ion channel in the pain pathway. Nature 389: 816-824. -   Caterina-M J. Leffler-A. Malmberg-A B. Martin-W J. Trafton-J.     Petersen-Zeitz K R. Koltzenburg-M. Basbaum-A I. Julius-D (2000)     Impaired nociception and pain sensation in mice lacking the     capsaicin receptor. Science-(WASH-DC). 288: 5464: 306-313. -   Cortright-D N. Crandall-M. Sanchez-J F. Zou-T. Krause-J E.     White-G (2001) The tissue distribution and functional     characterization of human VR1. Biochemical and Biophysical Research     Communications 281: 5: 1183-1189 Dray, A., (1992). Therapeutic     potential of capsaicin-like molecules. Life Sciences 51: 1759-1765. -   Gauldie-S D. McQueen-D S. Pertwee-R. Chessell-I P. (2001) Anandamide     activates peripheral nociceptors in normal and arthritic rat knee     joints. British Journal of Pharmacology 132: 3: 617-621. -   Helliwell-R J A. McLatchie-L M. Clarke-M. Winter-J. Bevan-S.     McIntyre-P (1998) Capsaicin sensitivity is associated with     expression of the vanilloid (capsaicin) receptor (VR1) mRNA in adult     rat sensory ganglia. Neuroscience Lett. 250: 3: 177-180. -   Holzer, P. (1991) Capsaicin: Cellular targets, Mechanisms of Action     and selectivity for thin sensory neurons. Pharmacological reviews     43: 2: 143-201 Hwang-S W. Cho-H. Kwak-J. Lee-S Y. Kang-C J. Jung-J.     Cho-S. -   Min-K H. Suh-Y G. Kim-D. Oh-U. (2000) Direct activation of capsaicin     receptors by products of lipoxygenases: Endogenous capsaicin-like     substances. PNAS 97: 11: 6155-6160. -   Mezey-E. Toth-Z E. Cortright-D N. Arzubi-M K. Krause-J E. Elde-R.     Guo-A. Blumberg-P M. Szallasi-A (2000) Distribution of mRNA for     vanilloid receptor subtype 1 (VR1), and VR1-like immunoreactivity,     in the central nervous system of the rat and human. -   PNAS 97: 7: 3655-3660. -   Nozawa-Y. Nishihara-K. Yamamoto-A. Nakano-M. Ajioka-H.     Matsuura-N. (2001) Distribution and characterization of vanilloid     receptors in the rat stomach. Neuroscience Letters 309: 1: 33-36. -   Olah-Z. Karai-L. Iadarola-M J. (2001) Anandamide activates vanilloid     receptor 1 (VR1) at acidic pH in dorsal root ganglia neurons and     cells ectopically expressing VR1. Journal of Biological Chemistry     276: 33, 31163-31170. -   Onozawa-K. Nakamura-A. Tsutsumi-S. Yao-J. Ishikawa-R.     Kohama-K. (2000) Tissue distribution of capsaicin receptor in the     various organs of rats. Proc. Jpn. Acad. Ser. B, Phys.-Biol. Sci.     76: 5: 68-72. -   Premkumar-L S. Ahern-G P. (2000) Induction of vanilloid receptor     channel activity by protein kinase C. Nature (London) 408: 6815:     985-990. -   Singh-L K. Pang-X. Alexacos-N. Letourneau-R. Theoharides-T C. (1999)     Acute immobilization stress triggers skin mast cell degranulation     via corticotropin releasing hormone, neurotensin, and substance P: A     link to neurogenic skin disorders. Brain Behav. Immun. 13: 3:     225-239. -   Szallasi, A. Blumberg-P M (1996) Vanilloid receptors: New insights     enhance potential as a therapeutic target. Pain 68: 195-208 -   Szallasi-A. Blumberg-P M. (1999) Vanilloid (capsaicin) receptors and     mechanisms. Pharmacol. Rev. 51: 2: 159-211. -   Szabo-T. Wang-J. Gonzalez-A. Kedei-N. Lile-J. Treanor-J.     Blumberg-P M. (2000) Pharmacological characterization of the human     vanilloid receptor type-1 (hVR1). Society for Neuroscience     Abstracts. 26:1-2: 634.18. -   Tominaga, M., Caterina, M. J., Malmberg, A. B., Rosen, T. A.,     Gilbert, H., Skinner, K., Raumann, B. E., Basbaum, A. I., and     Julius, D., (1998). The cloned capsaicin receptor integrates     multiple pain-producing stimuli. Neuron 21: 531-543. -   Yiangou-Y. Facer-P. Dyer-N H C. Chan-C L H. Knowles-C. -   Williams-N S. Anand-P. (2001) Vanilloid receptor 1 immunoreactivity     in inflamed human bowel. Lancet (North American Edition) 357: 9265:     1338-1339. -   Yiangou-Y. Facer-P. Ford-A. Brady-C. Wiseman-O. Fowler-C J.     Anand-P. (2001) Capsaicin receptor VR1 and ATP-gated ion channel     P2X3 in human urinary bladder. BJU International 87: 9: 774-779. -   Wang-H. Bian-D. Zhu-D. Zajic-G. Loeloff-R. Lile-J. Wild-K.     Treanor-J. Curran-E. (2000) Inflammation-induced upregulation of VR1     in rat spinal cord and DRG correlates with enhanced nociceptive     processing. Society for Neuroscience Abstracts 26:1-2: 632.15.

SUMMARY

The present invention comprises a new class of compounds useful in the treatment of diseases, such as vanilloid-receptor-mediated diseases and other maladies, such as inflammatory or neuropathic pain and diseases involving sensory nerve function such as asthma, rheumatoid arthritis, osteoarthritis, inflammatory bowel disorders, urinary incontinence, migraine and psoriasis. In particular, the compounds of the invention are useful for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders. Accordingly, the invention also comprises pharmaceutical compositions comprising the compounds, methods for the treatment of vanilloid-receptor-mediated diseases, such as inflammatory or neuropathic pain, asthma, rheumatoid arthritis, osteoarthritis, inflammatory bowel disorders, urinary incontinence, migraine and psoriasis diseases, using the compounds and compositions of the invention, and intermediates and processes useful for the preparation of the compounds of the invention.

The compounds of the invention are represented by the following general structure:

or a pharmaceutically acceptable salt thereof, wherein J, R¹, R⁴, R⁵, X and Y are defined below.

The foregoing merely summarizes certain aspects of the invention and is not intended, nor should it be construed, as limiting the invention in any way. All patents, patent applications and other publications recited herein are hereby incorporated by reference in their entirety.

DETAILED DESCRIPTION

One aspect of the current invention relates to compounds having the general structure:

or any pharmaceutically-acceptable salt or hydrate thereof, wherein:

J is NH, O, S, S(═O) or S(═O)₂;

X is N or C(R²);

Y is N or C(R³); wherein no more than one of X and Y is N;

n is independently, at each instance, 0, 1 or 2;

R¹ is a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 0, 1, 2 or 3 atoms selected from N, O and S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O) OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NROC₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I;

R² is selected from H, C₁₋₈alkyl, C₁₋₄haloalkyl, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c); or R² is a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 1, 2 or 3 atoms selected from N, O and S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 0, 1, 2 or 3 groups selected from R^(f), halo, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c); or R² is C₁₋₄alkyl substituted by 0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —C(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c);

R³ is

-   -   (A) H; or     -   (B) C₁₋₈alkyl substituted by 0, 1, 2 or 3 groups selected from         C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f),         —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g),         —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f),         —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f),         —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g),         —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g),         —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g),         —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g),         —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g),         —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c),         —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c),         —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c),         —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c),         —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c),         —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g),         —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g),         —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c),         —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g),         —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g),         —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(c),         —N(R^(a))C(═NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f),         —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g),         —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g),         —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and         —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2,         3, 4 or 5 substituents independently selected from Br, Cl, F and         I; or     -   (C) a saturated, partially saturated or unsaturated 5-, 6- or         7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered         bicyclic ring containing 1, 2 or 3 atoms selected from N, O and         S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo         groups, wherein the ring is substituted by 0, 1, 2 or 3 groups         selected from R^(f), halo, cyano, nitro, —C(═O)R^(f),         —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g),         —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g).         —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g),         —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f),         —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g),         —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g),         —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g),         —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g),         —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g),         —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c),         —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c),         —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c),         —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c),         —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c),         —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g),         —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g),         —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c),         —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g),         —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g),         —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g),         —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f),         —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g),         —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g),         —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and         —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2,         3, 4 or 5 substituents independently selected from Br, Cl, F and         I; or     -   (D) —N(R^(a))—C₁₋₈alkyl, wherein the C₁₋₈alkyl is substituted by         0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano,         nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g),         —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g),         —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g),         —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f),         —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g),         —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g),         —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g),         —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g),         —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g),         —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c),         —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c),         —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c),         —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c),         —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c),         —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g),         —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g),         —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c),         —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g),         —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g),         —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g),         —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f),         —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g),         —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g),         —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and         —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2,         3, 4 or 5 substituents independently selected from Br, Cl, F and         I; or     -   (D) —OC₁₋₈alkyl, wherein the C₁₋₈alkyl is substituted by 0, 1, 2         or 3 groups selected from C₁₋₄-haloalkyl, halo, cyano, nitro,         —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g),         —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f),         —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f),         —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g),         —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g),         —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g),         —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g),         —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g),         —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c),         —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c),         —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c),         —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c),         —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c),         —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g),         —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g),         —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c),         —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g),         —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g),         —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a)NR^(a)R^(g),         —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f),         —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g),         —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(a)C₂₋₆alkylNR^(a)R^(g),         —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and         —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2,         3, 4 or 5 substituents independently selected from Br, Cl, F and         I; or     -   (E) halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g),         —C(═NR^(a))NR^(a)R^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g),         —OC(═O)N(R^(a))S(═O)₂R^(f), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f),         —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g),         —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g),         —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g),         —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —C(═O)R^(c),         —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c),         —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c),         —OC(═O)N(R^(c))S(═O)₂R^(f), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c),         —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f),         —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g),         —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g),         —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═O)R^(f),         —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c),         —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c),         —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c),         —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c),         —N(R^(c))S(═O)₂NR^(a)R^(g) and —N(R^(a))S(═O)₂NR^(a)R^(c), and         additionally substituted by 0, 1, 2, 3, 4 or 5 substituents         independently selected from Br, Cl, F and I;

R⁴ is phenyl, the phenyl being vicinally fused with a saturated, partially saturated or unsaturated 5- or 6-membered carbocyclic ring or a saturated, partially saturated or unsaturated 5- or 6-membered heterocyclic ring containing 1, 2 or 3 N atoms and 0 or 1 O or S atoms, wherein the phenyl and ring are substituted by 0, 1, 2 or 3 substituents independently selected from R^(c), oxo, R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; provided R⁴ is not 6-(2H-benzo[b][1,4]oxazin-3(4H)-one) or any substituted version thereof;

R⁵ is H or CH₃;

R^(a) is independently, at each instance, H or R^(b);

R^(b) is independently, at each instance, phenyl, benzyl or C₁₋₆alkyl, the phenyl, benzyl and C₁₋₆alkyl being substituted by 0, 1, 2 or 3 substituents selected from, C₁₋₄alkyl, C₁₋₃haloalkyl, —OC₁₋₄alkyl, —NH₂, —NHC₁₋₄alkyl and —N(C₁₋₄alkyl)C₁₋₄alkyl, and additionally substituted by 0, 1, 2, 3, 4, 5 or 6 substitutents independently selected from F, Cl, Br and I.

R^(c) is independently at each instance a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 0, 1, 2, 3 or 4 atoms selected from N, O and S, wherein the carbon atoms of the ring are substituted by 0, 1 or 2 oxo or thioxo groups, sulfur atoms of the ring are substituted by 0, 1 or 2 oxo groups, nitrogen atoms of the ring are substituted by 0 or 1 oxo groups, and the ring is substituted by 0, 1, 2 or 3 substituents selected from C₁₋₈alkyl, C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(b), —C(═O)OR^(b), —C(═O)NR^(a)R^(a), —C(═NR^(a))NR^(a)R^(a), —OR^(a), —OC(═O)R^(b), —OC(═O)NR^(a)R^(a), —OC(═O)N(R^(a))S(═O)₂R^(b), —OC₂₋₆alkylNR^(a)R^(a), —OC₂₋₆alkylOR^(a), —SR^(a), —S(═O)R^(b), —S(═O)₂R^(b), —S(═O)₂NR^(a)R^(a), —S(═O)₂N(R^(a))C(═O)R^(b), —S(═O)₂N(R^(a))C(═O)OR^(b), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(a), —NR^(a)R^(a), —N(R^(a))C(═O)R^(b), —N(R^(a))C(═O)OR^(b), —N(R^(a))C(═O)NR^(a)R^(a), —N(R^(a))C(═NR^(a))NR^(a)R^(a), —N(R^(a))S(═O)₂R^(b), —N(R^(a))S(═O)₂NR^(a)R^(a), —NR^(a)C₂₋₆alkylNR^(a)R^(a) and —NR^(a)C₂₋₆alkylOR^(a), and the ring is additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I;

R^(d) is independently at each instance C₁₋₈alkyl, C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(b), —C(═O)OR^(b), —C(═O)NR^(a)R^(a), —C(═NR^(a))NR^(a)R^(a), —OR^(a), —OC(═O)R^(b), —OC(═O)NR^(a)R^(a), —OC(═O)N(R^(a))S(═O)₂R^(b), —OC₂₋₆alkylNR^(a)R^(a), —OC₂₋₆alkylOR^(a), —SR^(a), —S(═O)R^(b), —S(═O)₂R^(b), —S(═O)₂NR^(a)R^(a), —S(═O)₂N(R^(a))C(═O)R^(b), —S(═O)₂N(R^(a))C(═O)OR^(b), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(a), —NR^(a)R^(a), —N(R^(a))C(═O)R^(b), —N(R^(a))C(═O)OR^(b), —N(R^(a))C(═O)NR^(a)R^(a), —N(R^(a))C(═NR^(a))NR^(a)R^(a), —N(R^(a))S(═O)₂R^(b), —N(R^(a))S(═O)₂NR^(a)R^(a), —NR^(a)C₂₋₆alkylNR^(a)R^(a) or —NR^(a)C₂₋₆alkylOR^(a);

R^(e) is independently at each instance R^(d) or H;

R^(f) is independently at each instance C₁₋₈alkyl substituted by 0, 1, 2 or 3 substituents independently selected from C₁₋₄haloalkyl, cyano, nitro, —C(═O)R^(b), —C(═O)OR^(b), C(═O)NR^(a)R^(a), C(═NR^(a))NR^(a)R^(a), —OR^(a), —OC(═O)R^(b), —OC(═O)NR^(a)R^(a), —OC(═O)N(R^(a))S(═O)₂R^(b), —OC₂₋₆alkylNR^(a)R^(a), —OC₂₋₆alkylOR^(a), —SR^(a), —S(═O)R^(b), —S(═O)₂R^(b), —S(═O)₂NR^(a)R^(a), —S(═O)₂N(R^(a))C(═O)R^(b), —S(═O)₂N(R^(a))C(═O)OR^(b), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(a), —NR^(a)R^(a), —N(R^(a))C(═O)R^(b), —N(R^(a))C(═O)OR^(b), —N(R^(a))C(═O)NR^(a)R^(a), —N(R^(a))C(═NR^(a))NR^(a)R^(a), —N(R^(a))S(═O)₂R^(b), —N(R^(a))S(═O)₂NR^(a)R^(a), —NR^(a)C₂₋₆alkylNR^(a)R^(a) and —NR^(a)C₂₋₆alkylOR^(a); and

additionally substituted by 0 or 1 saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic rings containing 0, 1, 2, 3 or 4 atoms selected from N, O and S, wherein the carbon atoms of the ring are substituted by 0, 1 or 2 oxo or thioxo groups, sulfur atoms of the ring are substituted by 0, 1 or 2 oxo groups, nitrogen atoms of the ring are substituted by 0 or 1 oxo groups, and the ring is substituted by 0, 1, 2 or 3 substituents selected from C₁₋₈alkyl, C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(b), —C(═O)OR^(b), C(═O)NR^(a)R^(a), C(═NR^(a))NR^(a)R^(a), —OR^(a), —OC(═O)R^(b), —C(═O)NR^(a)R^(a), —OC(═O)N(R^(a))S(═O)₂R^(b), —OC₂₋₆alkylNR^(a)R^(a), —OC₂₋₆alkylOR^(a), —SR^(a), —S(═O)R^(b), —S(═O)₂R^(b), —S(═O)₂NR^(a)R^(a), —S(═O)₂N(R^(a))C(═O)R^(b), —S(═O)₂N(R^(a))C(═O)OR^(b), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(a), —NR^(a)R^(a), —N(R^(a))C(═O)R^(b), —N(R^(a))C(═O)OR^(b), —N(R^(a))C(═O)NR^(a)R^(a), —N(R^(a))C(═NR^(a))NR^(a)R^(a), —N(R^(a))S(═O)₂R^(b), —N(R^(a))S(═O)₂NR^(a)R^(a), —NR^(a)C₂₋₆alkylNR^(a)R^(a) and —NR^(a)C₂₋₆alkylOR^(a); and the C₁₋₈alkyl and ring are additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; and

R^(g) is independently at each instance R^(e) or H.

In one embodiment, in conjunction with any one of the above and below embodiments, J is NH or O.

In one embodiment, in conjunction with any one of the above and below embodiments, J is NH.

In one embodiment, in conjunction with any one of the above and below embodiments, J is O.

In another embodiment, in conjunction with any one of the above and below embodiments, X is C(R²) and Y is N.

In another embodiment, in conjunction with any one of the above and below embodiments, X is N and Y is C(R³).

In another embodiment, in conjunction with any one of the above and below embodiments, R¹ is a heterocycle selected from the group of thiophene, pyrrole, 1,3-oxazole, 1,3-thiazol-4-yl, 1,3,4-oxadiazole, 1,3,4-thiadiazole, 1,2,3-oxadiazole, 1,2,3-thiadiazole, 1H-1,2,3-triazole, isothiazole, 1,2,4-oxadiazole, 1,2,4-thiadiazole, 1,2,3,4-oxatriazole, 1,2,3,4-thiatriazole, 1H-1,2,3,4-tetraazole, 1,2,3,5-oxatriazole, 1,2,3,5-thiatriazole, furan, imidazol-2-yl, benzimidazole, 1,2,4-triazole, isoxazole, pyrazol-3-yl, pyrazol-4-yl, pyrazol-5-yl, thiolane, pyrrolidine, tetrahydrofuran, 4,5-dihydrothiophene, 2-pyrroline, 4,5-dihydrofuran, pyridazine, pyrimidine, pyrazine, 1,2,3-triazine, 1,2,4-triazine, 1,3,5-triazine, pyridine, 2H-3,4,5,6-tetrahydropyran, thiane, 1,2-diazaperhydroine, 1,3-diazaperhydroine, piperazine, 1,3-oxazaperhydroine, morpholine, 1,3-thiazaperhydroine, 1,4-thiazaperhydroine, piperidine, 2H-3,4-dihydropyran, 2,3-dihydro-4H-thiin, 1,4,5,6-tetrahydropyridine, 2H-5,6-dihydropyran, 2,3-dihydro-6H-thiin, 1,2,5,6-tetrahydropyridine, 3,4,5,6-tetrahydropyridine, 4H-pyran, 4H-thiin, 1,4-dihydropyridine, 1,4-dithiane, 1,4-dioxane, 1,4-oxathiane, 1,2-oxazolidine, 1,2-thiazolidine, pyrazolidine, 1,3-oxazolidine, 1,3-thiazolidine, imidazolidine, 1,2,4-oxadiazolidine, 1,3,4-oxadiazolidine, 1,2,4-thiadiazolidine, 1,3,4-thiadiazolidine, 1,2,4-triazolidine, 2-imidazolin-1-yl, 2-imidazolin-2-yl, 3-imidazoline, 2-pyrazoline, 4-imidazoline, 2,3-dihydroisothiazole, 4,5-dihydroisoxazole, 4,5-dihydroisothiazole, 2,5-dihydroisoxazole, 2,5-dihydroisothiazole, 2,3-dihydroisoxazole, 4,5-dihydrooxazole, 2,3-dihydrooxazole, 2,5-dihydrooxazole, 4,5-dihydrothiazole, 2,3-dihydrothiazole, 2,5-dihydrothiazole, 1,3,4-oxathiazolidine, 1,4,2-oxathiazolidine, 2,3-dihydro-1H-[1,2,3]triazole, 2,5-dihydro-1H-[1,2,3]triazole, 4,5-dihydro-1H-[1,2,3]triazol-1-yl, 4,5-dihydro-1H-[1,2,3]triazol-3-yl, 4,5-dihydro-1H-[1,2,3]triazol-5-yl, 2,3-dihydro-1H-[1,2,4]triazole, 4,5-dihydro-1H-[1,2,4]triazole, 2,3-dihydro-[1,2,4]oxadiazole, 2,5-dihydro-[1,2,4]oxadiazole, 4,5-dihydro-[1,2,4]thiadiazole, 2,3-dihydro-[1,2,4]thiadiazole, 2,5-dihydro-[1,2,4]thiadiazole, 4,5-dihydro-[1,2,4]thiadiazole, 2,5-dihydro-[1,2,4]oxadiazole, 2,3-dihydro-[1,2,4]oxadiazole, 4,5-dihydro-[1,2,4]oxadiazole, 2,5-dihydro-[1,2,4]thiadiazole, 2,3-dihydro-[1,2,4]thiadiazole, 4,5-dihydro-[1,2,4]thiadiazole, 2,3-dihydro-[1,3,4]oxadiazole, 2,3-dihydro-[1,3,4]thiadiazole, [1,4,2]oxathiazole, [1,3,4]oxathiazole, 1,3,5-triazaperhydroine, 1,2,4-triazaperhydroine, 1,4,2-dithiazaperhydroine, 1,4,2-dioxazaperhydroine, 1,3,5-oxadiazaperhydroine, 1,2,5-oxadiazaperhydroine, 1,3,4-thiadiazaperhydroine, 1,3,5-thiadiazaperhydroine, 1,2,5-thiadiazaperhydroine, 1,3,4-oxadiazaperhydroine, 1,4,3-oxathiazaperhydroine, 1,4,2-oxathiazaperhydroine, 1,4,5,6-tetrahydropyridazine, 1,2,3,4-tetrahydropyridazine, 1,2,3,6-tetrahydropyridazine, 1,2,5,6-tetrahydropyrimidine, 1,2,3,4-tetrahydropyrimidine, 1,4,5,6-tetrahydropyrimidine, 1,2,3,6-tetrahydropyrazine, 1,2,3,4-tetrahydropyrazine, 5,6-dihydro-4H-[1,2]oxazine, 5,6-dihydro-2H-[1,2]oxazine, 3,6-dihydro-2H-[1,2]oxazine, 3,4-dihydro-2H-[1,2]oxazine, 5,6-dihydro-4H-[1,2]thiazine, 5,6-dihydro-2H-[1,2]thiazine, 3,6-dihydro-2H-[1,2]thiazine, 3,4-dihydro-2H-[1,2]thiazine, 5,6-dihydro-2H-[1,3]oxazine, 5,6-dihydro-4H-[1,3]oxazine, 3,6-dihydro-2H-[1,3]oxazine, 3,4-dihydro-2H-[1,3]oxazine, 3,6-dihydro-2H-[1,4]oxazine, 3,4-dihydro-2H-[1,4]oxazine, 5,6-dihydro-2H-[1,3]thiazine, 5,6-dihydro-4H-[1,3]thiazine, 3,6-dihydro-2H-[1,3]thiazine, 3,4-dihydro-2H-[1,3]thiazine, 3,6-dihydro-2H-[1,4]thiazine, 3,4-dihydro-2H-[1,4]thiazine, 1,2,3,6-tetrahydro-[1,2,4]triazine, 1,2,3,4-tetrahydro-[1,2,4]triazine, 1,2,3,4-tetrahydro-[1,3,5]triazine, 2,3,4,5-tetrahydro-[1,2,4]triazine, 1,4,5,6-tetrahydro-[1,2,4]triazine, 5,6-dihydro-[1,4,2]dioxazine, 5,6-dihydro-[1,4,2]dithiazine, 2,3-dihydro-[1,4,2]dioxazine, 3,4-dihydro-2H-[1,3,4]oxadiazine, 3,6-dihydro-2H-[1,3,4]oxadiazine, 3,4-dihydro-2H-[1,3,5]oxadiazine, 3,6-dihydro-2H-[1,3,5]oxadiazine, 5,6-dihydro-2H-[1,2,5]oxadiazine, 5,6-dihydro-4H-[1,2,5]oxadiazine, 3,4-dihydro-2H-[1,3,4]thiadiazine, 3,6-dihydro-2H-[1,3,4]thiadiazine, 3,4-dihydro-2H-[1,3,5]thiadiazine, 3,6-dihydro-2H-[1,3,5]thiadiazine, 5,6-dihydro-2H-[1,2,5]thiadiazine, 5,6-dihydro-4H-[1,2,5]thiadiazine, 5,6-dihydro-2H-[1,2,3]oxadiazine, 3,6-dihydro-2H-[1,2,5]oxadiazine, 5,6-dihydro-4H-[1,3,4]oxadiazine, 3,4-dihydro-2H-[1,2,5]oxadiazine, 5,6-dihydro-2H-[1,2,3]thiadiazine, 3,6-dihydro-2H-[1,2,5]thiadiazine, 5,6-dihydro-4H-[1,3,4]thiadiazine, 3,4-dihydro-2H-[1,2,5]thiadiazine, 5,6-dihydro-[1,4,3]oxathiazine, 5,6-dihydro-[1,4,2]oxathiazine, 2,3-dihydro-[1,4,3]oxathiazine, 2,3-dihydro-[1,4,2]oxathiazine, 3,4-dihydropyridine, 1,2-dihydropyridine, 5,6-dihydropyridine, 2H-pyran, 2H-thiin, 3,6-dihydropyridine, 2,3-dihydropyridazine, 2,5-dihydropyridazine, 4,5-dihydropyridazine, 1,2-dihydropyridazine, 1,4-dihydropyrimidin-1-yl, 1,4-dihydropyrimidin-4-yl, 1,4-dihydropyrimidin-5-yl, 1,4-dihydropyrimidin-6-yl, 2,3-dihydropyrimidine, 2,5-dihydropyrimidine, 5,6-dihydropyrimidine, 3,6-dihydropyrimidine, 5,6-dihydropyrazine, 3,6-dihydropyrazine, 4,5-dihydropyrazine, 1,4-dihydropyrazine, 1,4-dithiin, 1,4-dioxin, 2H-1,2-oxazine, 6H-1,2-oxazine, 4H-1,2-oxazine, 2H-1,3-oxazine, 4H-1,3-oxazine, 6H-1,3-oxazine, 2H-1,4-oxazine, 4H-1,4-oxazine, 2H-1,3-thiazine, 2H-1,4-thiazine, 4H-1,2-thiazine, 6H-1,3-thiazine, 4H-1,4-thiazine, 2H-1,2-thiazine, 6H-1,2-thiazine, 1,4-oxathiin, 2H,5H-1,2,3-triazine, 1H,4H-1,2,3-triazine, 4,5-dihydro-1,2,3-triazine, 1H,6H-1,2,3-triazine, 1,2-dihydro-1,2,3-triazine, 2,3-dihydro-1,2,4-triazine, 3H,6H-1,2,4-triazine, 1H,6H-1,2,4-triazine, 3,4-dihydro-1,2,4-triazine, 1H,4H-1,2,4-triazine, 5,6-dihydro-1,2,4-triazine, 4,5-dihydro-1,2,4-triazine, 2H,5H-1,2,4-triazine, 1,2-dihydro-1,2,4-triazine, 1H,4H-1,3,5-triazine, 1,2-dihydro-1,3,5-triazine, 1,4,2-dithiazine, 1,4,2-dioxazine, 2H-1,3,4-oxadiazine, 2H-1,3,5-oxadiazine, 6H-1,2,5-oxadiazine, 4H-1,3,4-oxadiazine, 4H-1,3,5-oxadiazine, 4H-1,2,5-oxadiazine, 2H-1,3,5-thiadiazine, 6H-1,2,5-thiadiazine, 4H-1,3,4-thiadiazine, 4H-1,3,5-thiadiazine, 4H-1,2,5-thiadiazine, 2H-1,3,4-thiadiazine, 6H-1,3,4-thiadiazine, 6H-1,3,4-oxadiazine, and 1,4,2-oxathiazine, wherein the heterocycle is optionally vicinally fused with a saturated, partially saturated or unsaturated 5-, 6- or 7-membered ring containing 0, 1 or 2 atoms independently selected from N, O and S; wherein any of the heterocycles are substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c).

Embodiment A: In another embodiment, in conjunction with any one of the above and below embodiments, R¹ is a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 1, 2 or 3 atoms selected from N, O and S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R¹ is a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic ring containing 1, 2 or 3 atoms selected from N, O and S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I.

Embodiment B: In another embodiment, in conjunction with any one of the above and below embodiments, R¹ is a pyridinyl or pyrimidinyl ring substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R¹ is a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic carbocyclic ring, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I.

Embodiment C: In another embodiment, in conjunction with any one of the above and below embodiments, R¹ is 4-tert-butylphenyl or 4-trifluoromethylphenyl substituted by 0, 1 or 2 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC₂₋₆alkylNR^(a)R^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R¹ is 4-tert-butylphenyl or 4-trifluoromethylphenyl substituted by 1 or 2 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R¹ is 4-tert-butylphenyl or 4-trifluoromethylphenyl.

In another embodiment, in conjunction with any one of the above and below embodiments, R² is selected from C₁₋₈alkyl, C₁₋₄haloalkyl, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c); or R^(c) is a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 1, 2 or 3 atoms selected from N, O and S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 0, 1, 2 or 3 groups selected from R^(f), halo, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), ·OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c); or R² is C₁₋₄alkyl substituted by 0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c).

In another embodiment, in conjunction with any one of the above and below embodiments, R² is selected from H.

In another embodiment, in conjunction with any one of the above and below embodiments, R² is selected from C₁₋₈alkyl, C₁₋₄haloalkyl, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), ·OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c).

In another embodiment, in conjunction with any one of the above and below embodiments, R² is a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 1, 2 or 3 atoms selected from N, O and S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 0, 1, 2 or 3 groups selected from R^(f), halo, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c).

In another embodiment, in conjunction with any one of the above and below embodiments, R² is C₁₋₄alkyl substituted by 0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c).

In another embodiment, in conjunction with any one of the above and below embodiments, R³ is H.

In another embodiment, in conjunction with any one of the above and below embodiments, R³ is C₁₋₈alkyl substituted by 0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R³ is a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 1, 2 or 3 atoms selected from N, O and S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 0, 1, 2 or 3 groups selected from R^(f), halo, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a) C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R³ is —N(R^(a))—C₁₋₈alkyl, wherein the C₁₋₈alkyl is substituted by 0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆-alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R³ is —OC₁₋₈alkyl, wherein the C₁₋₈alkyl is substituted by 0, 1, 2 or 3 groups selected from CIhaloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R³ is halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g) and —N(R^(a))S(═O)₂NR^(a)R^(c), and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I.

Embodiment D: In another embodiment, in conjunction with any one of the above and below embodiments, R⁴ is phenyl, the phenyl being vicinally fused with a saturated, partially saturated or unsaturated 5- or 6-membered heterocyclic ring containing 1, 2 or 3 N atoms and 0 or 1 O or S atoms, wherein the phenyl and ring are substituted by 0, 1, 2 or 3 substituents independently selected from R^(c), oxo, R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; provided R⁴ is not 6-(2H-benzo[b][1,4]oxazin-3(4H)-one) or any substituted version thereof.

In another embodiment, in conjunction with any one of the above and below embodiments, R⁴ is phenyl, the phenyl being vicinally fused with a saturated, partially saturated or unsaturated 5- or 6-membered heterocyclic ring containing 1, 2 or 3 N atoms and 0 or 1 O or S atoms, wherein the phenyl and ring are substituted by 0, 1, 2 or 3 substituents independently selected from R^(c), R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —N^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I.

Embodiment E: In another embodiment, in conjunction with any one of the above and below embodiments, R⁴ is phenyl, the phenyl being vicinally fused with a saturated, partially saturated or unsaturated 5- or 6-membered heterocyclic ring containing 1, 2 or 3 N atoms and 0 or 1 S atoms, wherein the phenyl and ring are substituted by 0, 1, 2 or 3 substituents independently selected from R^(c), oxo, R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R⁴ is phenyl, the phenyl being vicinally fused with a saturated, partially saturated or unsaturated 5- or 6-membered carbocyclic ring or a saturated, partially saturated or unsaturated 5- or 6-membered heterocyclic ring containing 1, 2 or 3 N atoms and 0 or 1 O or S atoms, wherein the phenyl and ring are substituted by 0, 1, 2 or 3 substituents independently selected from R^(c), oxo, R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(c), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; provided when the R⁴ ring contains only one N atom and only one O atom, the ring is not substitued by oxo.

Embodiment F: In another embodiment, in conjunction with any one of the above and below embodiments, R⁴ is phenyl, the phenyl being vicinally fused with a saturated, partially saturated or unsaturated 5- or 6-membered heterocyclic ring containing 1, 2 or 3 N atoms, wherein the phenyl and ring are substituted by 0, 1, 2 or 3 substituents independently selected from R^(c), oxo, R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I.

Embodiment G: In another embodiment, in conjunction with any one of the above and below embodiments, R⁴ is phenyl, the phenyl being vicinally fused with a saturated, partially saturated or unsaturated 5- or 6-membered carbocyclic ring, wherein the phenyl and ring are substituted by 0, 1, 2 or 3 substituents independently selected from R^(c), oxo, R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I.

In another embodiment, in conjunction with any one of the above and below embodiments, R⁵ is H.

As stated above, the above embodiments may be used in conjuction with other embodiments listed. The following table is a non-exclusive, non-limiting list of some of the combinations of embodiments. Wherein J is NH, Y is CH and X is N:

Emb. # R¹ R⁴ 1001 A D 1002 B D 1003 C D 1004 A E 1005 B E 1006 C E 1007 A F 1008 B F 1009 C F 1010 A G 1011 B G 1012 C G Wherein J is O, Y is CH and X is N:

Emb. # R¹ R⁴ 2001 A D 2002 B D 2003 C D 2004 A E 2005 B E 2006 C E 2007 A F 2008 B F 2009 C F 2010 A G 2011 B G 2012 C G

Another aspect of the invention relates to a method of treating acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodyia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neurophathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, gastroesophageal reflux disease, effective disorder, depression, anxiety, wounds, burns, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders, comprising the step of administering a compound according to any of the above embodiments.

Another aspect of the invention relates to a pharmaceutical composition comprising a compound according to any of the above embodiments and a pharmaceutically-acceptable diluent or carrier.

Another aspect of the invention relates to the use of a compound according to any of the above embodiments as a medicament.

Another aspect of the invention relates to the use of a compound according to any of the above embodiments in the manufacture of a medicament for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.

Another aspect of the invention relates to a method of making a compound according to the above embodiments, comprising the step of:

reacting

with R¹JH to form

The compounds of this invention may have in general several asymmetric centers and are typically depicted in the form of racemic mixtures. This invention is intended to encompass racemic mixtures, partially racemic mixtures and separate enantiomers and diasteromers.

Unless otherwise specified, the following definitions apply to terms found in the specification and claims:

“C_(α-β)alkyl” means an alkyl group comprising a minimum of α and a maximum of β carbon atoms in a branched, cyclical or linear relationship or any combination of the three, wherein α and β represent integers. The alkyl groups described in this section may also contain one or two double or triple bonds. Examples of C₁₋₆alkyl include, but are not limited to the following:

“Benzo group”, alone or in combination, means the divalent radical C₄H₄═, one representation of which is —CH═CH—CH═CH—, that when vicinally attached to another ring forms a benzene-like ring—for example tetrahydronaphthylene, indole and the like. The terms “oxo” and “thioxo” represent the groups=O (as in carbonyl) and =S (as in thiocarbonyl), respectively. “Halo” or “halogen” means a halogen atoms selected from F, Cl, Br and I. “C_(V-W)haloalkyl” means an alkyl group, as described above, wherein any number—at least one—of the hydrogen atoms attached to the alkyl chain are replaced by F, Cl, Br or I. “Heterocycle” means a ring comprising at least one carbon atom and at least one other atom selected from N, O and S. Examples of heterocycles that may be found in the claims include, but are not limited to, the following:

“Available nitrogen atoms” are those nitrogen atoms that are part of a heterocycle and are joined by two single bonds (e.g. piperidine), leaving an external bond available for substitution by, for example, H or CH₃. “Pharmaceutically-acceptable salt” means a salt prepared by conventional means, and are well known by those skilled in the art. The “pharmacologically acceptable salts” include basic salts of inorganic and organic acids, including but not limited to hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, malic acid, acetic acid, oxalic acid, tartaric acid, citric acid, lactic acid, fumaric acid, succinic acid, maleic acid, salicylic acid, benzoic acid, phenylacetic acid, mandelic acid and the like. When compounds of the invention include an acidic function such as a carboxy group, then suitable pharmaceutically acceptable cation pairs for the carboxy group are well known to those skilled in the art and include alkaline, alkaline earth, ammonium, quaternary ammonium cations and the like. For additional examples of “pharmacologically acceptable salts,” see infra and Berge et al., J. Pharm. Sci. 66:1 (1977). “Saturated or unsaturated” includes substituents saturated with hydrogens, substituents completely unsaturated with hydrogens and substituents partially saturated with hydrogens. “Leaving group” generally refers to groups readily displaceable by a nucleophile, such as an amine, a thiol or an alcohol nucleophile. Such leaving groups are well known in the art. Examples of such leaving groups include, but are not limited to, N-hydroxysuccinimide, N-hydroxybenzotriazole, halides, triflates, tosylates and the like. Preferred leaving groups are indicated herein where appropriate. “Protecting group” generally refers to groups well known in the art which are used to prevent selected reactive groups, such as carboxy, amino, hydroxy, mercapto and the like, from undergoing undesired reactions, such as nucleophilic, electrophilic, oxidation, reduction and the like. Preferred protecting groups are indicated herein where appropriate. Examples of amino protecting groups include, but are not limited to, aralkyl, substituted aralkyl, cycloalkenylalkyl and substituted cycloalkenyl alkyl, allyl, substituted allyl, acyl, alkoxycarbonyl, aralkoxycarbonyl, silyl and the like. Examples of aralkyl include, but are not limited to, benzyl, ortho-methylbenzyl, trityl and benzhydryl, which can be optionally substituted with halogen, alkyl, alkoxy, hydroxy, nitro, acylamino, acyl and the like, and salts, such as phosphonium and ammonium salts. Examples of aryl groups include phenyl, naphthyl, indanyl, anthracenyl, 9-(9-phenylfluorenyl), phenanthrenyl, durenyl and the like. Examples of cycloalkenylalkyl or substituted cycloalkylenylalkyl radicals, preferably have 6-10 carbon atoms, include, but are not limited to, cyclohexenyl methyl and the like. Suitable acyl, alkoxycarbonyl and aralkoxycarbonyl groups include benzyloxycarbonyl, t-butoxycarbonyl, iso-butoxycarbonyl, benzoyl, substituted benzoyl, butyryl, acetyl, trifluoroacetyl, trichloro acetyl, phthaloyl and the like. A mixture of protecting groups can be used to protect the same amino group, such as a primary amino group can be protected by both an aralkyl group and an aralkoxycarbonyl group. Amino protecting groups can also form a heterocyclic ring with the nitrogen to which they are attached, for example, 1,2-bis(methylene)benzene, phthalimidyl, succinimidyl, maleimidyl and the like and where these heterocyclic groups can further include adjoining aryl and cycloalkyl rings. In addition, the heterocyclic groups can be mono-, di- or tri-substituted, such as nitrophthalimidyl. Amino groups may also be protected against undesired reactions, such as oxidation, through the formation of an addition salt, such as hydrochloride, toluenesulfonic acid, trifluoroacetic acid and the like. Many of the amino protecting groups are also suitable for protecting carboxy, hydroxy and mercapto groups. For example, aralkyl groups. Alkyl groups are also suitable groups for protecting hydroxy and mercapto groups, such as tert-butyl.

Silyl protecting groups are silicon atoms optionally substituted by one or more alkyl, aryl and aralkyl groups. Suitable silyl protecting groups include, but are not limited to, trimethylsilyl, triethylsilyl, triisopropylsilyl, tert-butyldimethylsilyl, dimethylphenylsilyl, 1,2-bis(dimethylsilyl)benzene, 1,2-bis(dimethylsilyl)ethane and diphenylmethylsilyl. Silylation of an amino groups provide mono- or di-silylamino groups. Silylation of aminoalcohol compounds can lead to a N,N,O-trisilyl derivative. Removal of the silyl function from a silyl ether function is readily accomplished by treatment with, for example, a metal hydroxide or ammonium fluoride reagent, either as a discrete reaction step or in situ during a reaction with the alcohol group. Suitable silylating agents are, for example, trimethylsilyl chloride, tert-butyl-dimethylsilyl chloride, phenyldimethylsilyl chloride, diphenylmethyl silyl chloride or their combination products with imidazole or DMF. Methods for silylation of amines and removal of silyl protecting groups are well known to those skilled in the art. Methods of preparation of these amine derivatives from corresponding amino acids, amino acid amides or amino acid esters are also well known to those skilled in the art of organic chemistry including amino acid/amino acid ester or aminoalcohol chemistry.

Protecting groups are removed under conditions which will not affect the remaining portion of the molecule. These methods are well known in the art and include acid hydrolysis, hydrogenolysis and the like. A preferred method involves removal of a protecting group, such as removal of a benzyloxycarbonyl group by hydrogenolysis utilizing palladium on carbon in a suitable solvent system such as an alcohol, acetic acid, and the like or mixtures thereof. A t-butoxycarbonyl protecting group can be removed utilizing an inorganic or organic acid, such as HCl or trifluoroacetic acid, in a suitable solvent system, such as dioxane or methylene chloride. The resulting amino salt can readily be neutralized to yield the free amine. Carboxy protecting group, such as methyl, ethyl, benzyl, tert-butyl, 4-methoxyphenylmethyl and the like, can be removed under hydrolysis and hydrogenolysis conditions well known to those skilled in the art.

It should be noted that compounds of the invention may contain groups that may exist in tautomeric forms, such as cyclic and acyclic amidine and guanidine groups, heteroatom substituted heteroaryl groups (Y′=O, S, NR), and the like, which are illustrated in the following examples:

and though one form is named, described, displayed and/or claimed herein, all the tautomeric forms are intended to be inherently included in such name, description, display and/or claim.

Prodrugs of the compounds of this invention are also contemplated by this invention. A prodrug is an active or inactive compound that is modified chemically through in vivo physiological action, such as hydrolysis, metabolism and the like, into a compound of this invention following administration of the prodrug to a patient. The suitability and techniques involved in making and using prodrugs are well known by those skilled in the art. For a general discussion of prodrugs involving esters see Svensson and Tunek Drug Metabolism Reviews 165 (1988) and Bundgaard Design of Prodrugs, Elsevier (1985). Examples of a masked carboxylate anion include a variety of esters, such as alkyl (for example, methyl, ethyl), cycloalkyl (for example, cyclohexyl), aralkyl (for example, benzyl, p-methoxybenzyl), and alkylcarbonyloxyalkyl (for example, pivaloyloxymethyl). Amines have been masked as arylcarbonyloxymethyl substituted derivatives which are cleaved by esterases in vivo releasing the free drug and formaldehyde (Bungaard J. Med. Chem. 2503 (1989)). Also, drugs containing an acidic NH group, such as imidazole, imide, indole and the like, have been masked with N-acyloxymethyl groups (Bundgaard Design of Prodrugs, Elsevier (1985)). Hydroxy groups have been masked as esters and ethers. EP 039,051 (Sloan and Little, Apr. 11, 1981) discloses Mannich-base hydroxamic acid prodrugs, their preparation and use.

The specification and claims contain listing of species using the language “selected from . . . and . . . ” and “is . . . or . . . ” (sometimes referred to as Markush groups). When this language is used in this application, unless otherwise stated it is meant to include the group as a whole, or any single members thereof, or any subgroups thereof. The use of this language is merely for shorthand purposes and is not meant in any way to limit the removal of individual elements or subgroups as needed.

Experimental

Unless otherwise noted, all materials were obtained from commercial suppliers and used without further purification. All parts are by weight and temperatures are in degrees centigrade unless otherwise indicated. All microwave assisted reactions were conducted with a Smith Synthesizer from Personal Chemistry, Uppsala, Sweden. All compounds showed NMR spectra consistent with their assigned structures. Melting points were determined on a Buchi apparatus and are uncorrected. Mass spectral data was determined by electrospray ionization technique. All examples were purified to >90% purity as determined by high-performance liquid chromatography. Unless otherwise stated, reactions were run at room temperature.

The following abbreviations are used:

-   -   DMSO—dimethyl sulfoxide     -   DMF—N,N-dimethylformamide     -   THF—tetrahydrofuran     -   Et₂O—diethyl ether     -   EtOAc—ethyl acetate     -   MeOH—methyl alcohol     -   EtOH—ethyl alcohol     -   MeCN—acetonitrile     -   MeI—iodomethane     -   MP—CO₃—macroporous carbonate     -   NMP—1-methyl-2-pyrrolidinone     -   DCM—dichloromethane     -   TFA—trifuoroacetic acid     -   Sat.—saturated     -   h—hour     -   min—minutes     -   mL milliliters     -   g grams     -   mg milligrams         Generic Schemes         Generic Schemes for the preparation of pyridine core (I):

Generic Schemes for the Preparation of Pyrimidine Core (II):

Generic Schemes for the Preparation of Pyridazine Core (III):

EXAMPLE 1

6-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-N-(4-(trifluoromethyl)phenyl)pyrimidin-4-amine

(a) 6-Chloro-N-(4-(trifluoromethyl)phenyl)pyrimidin-4-amine. A mixture of 4,6-dichloropyrimidine (Aldrich, 5.11 g, 34.3 mmol) and 4-trifluoromethylaniline (Aldrich, 5.52 g, 34.3 mmol) in 100 mL isopropanol was heated to 80° C. After 18 h the reaction was allowed to cool to room temperature and the resulting precipitate was filtered, washed consecutively with cold isopropanol and pentane and dried in vacuo to give a white crystalline solid. MS (ESI, pos ion.) m/z: 274 (M+1).

(b) 6-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-N-(4-(trifluoromethyl)phenyl)-pyrimidin-4-amine. A mixture of 6-chloro-N-(4-(trifluoromethyl)phenyl)-pyrimidin-4-amine (273 mg, 1.0 mmol), 2.3-dihydro-1,4-benzodioxin-6-ylboronic acid (Maybridge, 200 mg, 1.1 mmol), Na₂CO₃ (433 mg, 4.1 mmol) and Pd(PPh₃)₄ (Strem, 115 mg, 0.1 mmol) in 8 mL DME/3 mL H₂O was heated to 90° C. After 3.5 h the reaction was cooled to room temperature and partitioned between EtOAc/brine. The aqueous layer was extracted with EtOAc (3×) and the combined organics were dried over Na₂SO₄. The solution was filtered, evaporated onto SiO₂ and purified by flash column chromatography eluting with EtOAc/Hex (0-25%) to give a light yellow amorphous solid. MS (ESI, pos ion.) m/z: 374 (M+1).

Additional Examples

Following the procedure described above for Example 1b, or with slight modifications thereof, the following examples were prepared:

Ex- am- MS (ESI, ple Structure posion.) m/z: 2

367 (M + 1) 3

367 (M + 1) 4

355 (M + 1) 5

367 (M + 1) 6

388 (M + 1) 7

358 (M + 1) 8

367 (M + 1)

EXAMPLE 9

6-(Quinoxalin-6-yl)-N-(4-(trifluoromethyl)phenyl)pyrimidin-4-amine. A mixture of 6-chloro-N-(4-(trifluoromethyl)phenyl)pyrimidin-4-amine (273 mg, 1.0 mmol), benzopyrazine-6-boronic acid hydrochloride (Asymchem, 211 mg, 1.0 mmol), Na₂CO₃ (529 mg, 5.0 mmol) and PdCl₂(PPh₃)₂ (Strem, 60 mg, 0.1 mmol) in 7 mL DME/3 mL H₂O/2 mL EtOH was heated to 120° C. for 17 min in the Smith Optimizer microwave. The reaction mixture was partitioned between EtOAc/brine and the aqueous layer was extracted with EtOAc (3×). The combined organics were evaporated onto SiO₂ and purified by flash column chromatography eluting with EtOAc/Hexane/2M NH₃ in MeOH/CH₂Cl₂ (0:1:0:0→1:1:0:0→0:0:19:1). The fractions containing desired compound were combined and concentrated in vacuo giving a solid. The solid was washed with a minimal amount of CH₂Cl₂ and dried in vacuo to give a light pink amorphous solid. MS (ESI, pos ion.) m/z: 368 (M+1).

EXAMPLE 10

(a) Quinolin-7-ylboronic acid. A mixture of 7-aminoquinoline (4.02 g, 27.9 mmol), CsI (Aldrich, 7.32 g, 28.2 mmol), iodine (Aldrich, 5.71 g, 22.5 mmol), CuI (Aldrich, 2.67 g, 14.0 mmol) and isoamyl nitrite (Aldrich, 22 mL, 19.18 g, 163.7 mmol) in 200 mL DME was heated to 60° C. After 2 h the reaction was cooled to room temperature and filtered. The filtrate was diluted with 300 mL toluene and washed consecutively with 25% NH₄OH (2×100 mL), 5% Na₂S₂O₃ (2×100 mL) and 5% NaCl (2×100 mL). The organic solution was dried over Na₂SO₄, evaporated onto SiO₂ and purified by flash column chromatography eluting with EtOAc/Hex (0-25%) to give 7-iodoquinoline. MS (ESI, pos ion.) m/z: 256 (M+1). To a cooled (−78° C.) solution of the above 7-iodoquinoline (2.66 g, 10.4 mmol) in 20 mL THF was added 2.5M n-BuLi (5.0 mL, 12.5 mmol) drop-wise over 20 min. After an additional 20 min, B(OMe)₃ (Aldrich, 3.0 mL, 26.9 mmol) was added dropwise and the reaction was warmed to room temperature. After 4 h the reaction was cooled to −78° C. and 2.5M n-BuLi (5.0 mL, 12.5 mmol) was added and the mixture allowed to warm to room temperature. After 2 h 2.5M HCl (40 mL) was added and the mixture washed with Et₂O. The aqueous layer was neutralized with solid NaHCO₃, extracted with 10% i-PrOH/EtOAc and the solvent removed in vacuo to give a rust colored amorphous solid. MS (ESI, pos ion). m/z: 174 (M+1).

(b) 6-(Quinolin-7-yl)-N-(4-(trifluoromethyl)phenyl)pyrimidin-4-amine. The title compound was prepared analogous to the procedure used to prepare Example 1b, using 6-chloro-N-(4-(trifluoromethyl)phenyl)pyrimidin-4-amine (271 mg, 1.0 mmol), quinoline-7-boronic acid (193 mg, 1.1 mmol), Na₂CO₃ (472 mg, 4.1 mmol) and Pd(PPh₃)₄ (Strem, 104 mg, 0.1 mmol) in 8 mL DME/3 mL H₂O. Heating to 83° C. for 3 h gave an off-white amorphous solid. MS (ESI, pos ion.) m/z: 367 (M+1).

EXAMPLE 11

(7-(6-(4-(Trifluoromethyl)phenoxy)pyrimidin-4-yl)quinoline.

(a) 4-Chloro-6-(4-(trifluoromethyl)phenoxy)pyrimidine. A mixture of 4,6-di-chloropyrimidine (450 mg, 3 mmol, Aldrich), 4-(trifluoromethyl)phenol (486 mg, 3 mmol, Aldrich) and MP—CO₃ (1.3 g, 3.5 mmol, Argonaut Technologies) in DCM (10 mL) was heated to 100° C. in a microwave synthesizer for 5 min. The reaction mixture was allowed to cool to room temperature, filtered and washed with MeOH. The solvent removed in vacuo, and the residue purified by silica gel chromatography, DCM/MeOH (2%) to give the title compound as a white amorphous solid. MS (ESI, pos. ion) m/z: 275.1 (M+1).

(b) 7-(6-(4-(Trifluoromethyl)phenoxy)pyrimidin-4-yl)quinoline. A mixture of 4-chloro-6-(4-(trifluoromethyl)phenoxy)pyrimidine (274 mg, 1 mmol), quinolin-7-ylboronic acid (173 mg, 1 mmol, Example 10a), tetrakis(triphenylphosphine)-palladium(0) (50 mg, 0.04 mmol, Strem), aqueous sodium carbonate (1 mL, 2 mmol) in dioxane (4 mL) was heated to 150° C. in a microwave synthesizer for 5 min. The reaction mixture was allowed to cool to room temperature, filtered through Celite™, washed with ethyl acetate. The solvent removed in vacuo and the residue purified by silica gel chromatography, DCM/MeOH (2%) to give the title compound as an off white solid. MS (ESI, pos. ion) m/z: 368.1 (M+1). Biological Assays: Capsaicin-Induced Ca2+ Influx in Primary Dorsal Root Ganglion Neurons Embryonic 19 day old (E19) dorsal root ganglia (DRG) were dissected from timed-pregnant, terminally anesthetized Sprague-Dawley rats (Charles River, Wilmington, Mass.) and collected in ice-cold L-15 media (Life Technologies, Grand Island, N.Y.) containing 5% heat inactivated horse serum (Life Technologies). The DRG were then dissociated into single cell suspension using a papain dissociation system (Worthington Biochemical Corp., Freehold, N.J.). The dissociated cells were pelleted at 200×g for 5 min and re-suspended in EBSS containing 1 mg/ml ovomucoid inhibitor, 1 mg/ml ovalbumin and 0.005% DNase. Cell suspension was centrifuged through a gradient solution containing 10 mg/ml ovomucoid inhibitor, 10 mg/ml ovalbumin at 200×g for 6 min to remove cell debris; and filtered through a 88-μm nylon mesh (Fisher Scientific, Pittsburgh, Pa.) to remove any clumps. Cell number was determined with a hemocytometer and cells were seeded into poly-ornithine 100 μg/ml (Sigma) and mouse laminin 1 μg/ml (Life Technologies)-coated 96-well plates at 10×10³ cells/well in complete medium. The complete medium consists of minimal essential medium (MEM) and Ham's F 12, 1:1, penicillin (100 U/ml), and streptomycin (100 μg/ml), and nerve growth factor (10 ng/ml), 10% heat inactivated horse serum (Life Technologies). The cultures were kept at 37° C., 5% CO₂ and 100% humidity. For controlling the growth of non-neuronal cells, 5-fluoro-2′-deoxyuridine (75 μM) and uridine (180 μM) were included in the medium. Activation of VR1 is achieved in these cellular assays using either a capsaicin stimulus (ranging from 0.01-10 μM) or by an acid stimulus (addition of 30 mM Hepes/Mes buffered at pH 4.1). Compounds are also tested in an assay format to evaluate their agonist properties at VR1. Capsaicin Antagonist Assay: E-19 DRG cells at 5 days in culture are incubated with serial concentrations of VR1 antagonists, in HBSS (Hanks buffered saline solution supplemented with BSA 0.1 mg/ml and 1 mM Hepes at pH 7.4) for 15 min, 37° C. Cells are then challenged with a VR1 agonist, capsaicin 200 nM, in activation buffer containing 0.1 mg/ml BSA, 15 mM Hepes, pH 7.4, and 10 μCi/ml ⁴⁵Ca²⁺ (Amersham) in Ham's F12 for 2 min at 37° C. Acid Antagonist Assay: Compounds are pre-incubated with E-19 DRG cells for 2 minutes prior to addition of Calcium-45 in 30 mM Hepes/Mes buffer (Final Assay pH 5) and then left for an additional 2 minutes prior to compound washout. Final 45Ca (Amersham CES3-2 mCi) at 10 μCi/mL. Agonist Assay: Compounds are incubated with E-19 DRG cells for 2 minutes in the presence of Calcium-45 prior to compound washout. Final ⁴⁵Ca²⁺ (Amersham CES3-2 mCi) at 10 μCi/mL. Compound Washout and Analysis: Assay plates are washed using an ELX405 plate washer (Bio-Tek Instruments Inc.) immediately after functional assay. Wash 3× with PBS Mg2+/Ca2+ free, 0.1 mg/mL BSA. Aspirate between washes. Read plates using a MicroBeta Jet (Wallac Inc.). Compound activity is then calculated using appropriate computational algorithms. ⁴⁵Calcium²⁺ Assay Protocol Compounds may be assayed using Chinese Hamster Ovary cell lines stably expressing either human VR1 or rat VR1 under a CMV promoter. Cells can be cultured in Growth Medium, routinely passaged at 70% confluency using trypsin and plated in the assay plate 24 hours prior to compound evaluation.

Possible Growth Medium:

DMEM, high glucose (Gibco 11965-084).

10% Dialyzed serum (Hyclone SH30079.03).

1× Non-Essential Amino Acids (Gibco 11140-050).

1× Glutamine-Pen-Strep (Gibco 10378-016).

Geneticin, 450 μg/mL (Gibco 10131-035).

Compounds can be diluted in 100% DMSO and tested for activity over several log units of concentration [40 μM-2 pM]. Compounds may be further diluted in HBSS buffer (pH 7.4) 0.1 mg/mL BSA, prior to evaluation. Final DMSO concentration in assay would be 0.5%. Each assay plate can be controlled with a buffer only and a known antagonist compound (either capsazepine or one of the described VR1 antagonists).

Activation of VR1 can be achieved in these cellular assays using either a capsaicin stimulus (ranging from 0.1-1 μM) or by an acid stimulus (addition of 30 mM Hepes/Mes buffered at pH 4.1). Compounds may also tested in an assay format to evaluate their agonist properties at VR1.

Capsaicin Antagonist Assay: Compounds may be pre-incubated with cells (expressing either human or rat VR1) for 2 minutes prior to addition of Calcium-45 and Capsaicin and then left for an additional 2 minutes prior to compound washout. Capsaicin (0.5 nM) can be added in HAM's F12, 0.1 mg/mL BSA, 15 mM Hepes at pH 7.4. Final ⁴⁵Ca (Amersham CES3-2 mCi) at 10 μCi/mL. Acid Antagonist Assay: Compounds can be pre-incubated with cells (expressing either human or rat VR1) for 2 minutes prior to addition of Calcium-45 in 30 mM Hepes/Mes buffer (Final Assay pH 5) and then left for an additional 2 minutes prior to compound washout. Final ⁴⁵Ca (Amersham CES3-2 mCi) at 10 μCi/mL. Agonist Assay: Compounds can be incubated with cells (expressing either human or rat VR1) for 2 minutes in the presence of Calcium-45 prior to compound washout. Final ⁴⁵Ca (Amersham CES3-2 mCi) at 10 μCi/mL. Compound Washout and Analysis: Assay plates can be washed using an ELX405 plate washer (Bio-Tek Instruments Inc.) immediately after functional assay. One can wash 3× with PBS Mg2⁺/Ca²⁺ free, 0.1 mg/mL BSA, aspirating between washes. Plates may be read using a MicroBeta Jet (Wallac Inc.). Compound activity may then calculate using appropriate computational algorithms.

Useful nucleic acid sequences and proteins may be found in U.S. Pat. Nos. 6,335,180, 6,406,908 and 6,239,267, herein incorporated by reference in their entirety.

For the treatment of vanilloid-receptor-diseases, such as acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritus, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders, the compounds of the present invention may be administered orally, parentally, by inhalation spray, rectally, or topically in dosage unit formulations containing conventional pharmaceutically acceptable carriers, adjuvants, and vehicles. The term parenteral as used herein includes, subcutaneous, intravenous, intramuscular, intrastemal, infusion techniques or intraperitoneally.

Treatment of diseases and disorders herein is intended to also include the prophylactic administration of a compound of the invention, a pharmaceutical salt thereof, or a pharmaceutical composition of either to a subject (i.e., an animal, preferably a mammal, most preferably a human) believed to be in need of preventative treatment, such as, for example, pain, inflammation and the like.

The dosage regimen for treating vanilloid-receptor-mediated diseases, cancer, and/or hyperglycemia with the compounds of this invention and/or compositions of this invention is based on a variety of factors, including the type of disease, the age, weight, sex, medical condition of the patient, the severity of the condition, the route of administration, and the particular compound employed. Thus, the dosage regimen may vary widely, but can be determined routinely using standard methods. Dosage levels of the order from about 0.01 mg to 30 mg per kilogram of body weight per day, preferably from about 0.1 mg to 10 mg/kg, more preferably from about 0.25 mg to 1 mg/kg are useful for all methods of use disclosed herein.

The pharmaceutically active compounds of this invention can be processed in accordance with conventional methods of pharmacy to produce medicinal agents for administration to patients, including humans and other mammals.

For oral administration, the pharmaceutical composition may be in the form of, for example, a capsule, a tablet, a suspension, or liquid. The pharmaceutical composition is preferably made in the form of a dosage unit containing a given amount of the active ingredient. For example, these may contain an amount of active ingredient from about 1 to 2000 mg, preferably from about 1 to 500 mg, more preferably from about 5 to 150 mg. A suitable daily dose for a human or other mammal may vary widely depending on the condition of the patient and other factors, but, once again, can be determined using routine methods.

The active ingredient may also be administered by injection as a composition with suitable carriers including saline, dextrose, or water. The daily parenteral dosage regimen will be from about 0.1 to about 30 mg/kg of total body weight, preferably from about 0.1 to about 10 mg/kg, and more preferably from about 0.25 mg to 1 mg/kg.

Injectable preparations, such as sterile injectable aqueous or oleaginous suspensions, may be formulated according to the known are using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, for example as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed, including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid find use in the preparation of injectables.

Suppositories for rectal administration of the drug can be prepared by mixing the drug with a suitable non-irritating excipient such as cocoa butter and polyethylene glycols that are solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum and release the drug.

A suitable topical dose of active ingredient of a compound of the invention is 0.1 mg to 150 mg administered one to four, preferably one or two times daily. For topical administration, the active ingredient may comprise from 0.001% to 10% w/w, e.g., from 1% to 2% by weight of the formulation, although it may comprise as much as 10% w/w, but preferably not more than 5% w/w, and more preferably from 0.1% to 1% of the formulation.

Formulations suitable for topical administration include liquid or semi-liquid preparations suitable for penetration through the skin (e.g., liniments, lotions, ointments, creams, or pastes) and drops suitable for administration to the eye, ear, or nose.

For administration, the compounds of this invention are ordinarily combined with one or more adjuvants appropriate for the indicated route of administration. The compounds may be admixed with lactose, sucrose, starch powder, cellulose esters of alkanoic acids, stearic acid, talc, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphoric and sulfueric acids, acacia, gelatin, sodium alginate, polyvinyl-pyrrolidine, and/or polyvinyl alcohol, and tableted or encapsulated for conventional administration. Alternatively, the compounds of this invention may be dissolved in saline, water, polyethylene glycol, propylene glycol, ethanol, corn oil, peanut oil, cottonseed oil, sesame oil, tragacanth gum, and/or various buffers. Other adjuvants and modes of administration are well known in the pharmaceutical art. The carrier or diluent may include time delay material, such as glyceryl monostearate or glyceryl distearate alone or with a wax, or other materials well known in the art.

The pharmaceutical compositions may be made up in a solid form (including granules, powders or suppositories) or in a liquid form (e.g., solutions, suspensions, or emulsions). The pharmaceutical compositions may be subjected to conventional pharmaceutical operations such as sterilization and/or may contain conventional adjuvants, such as preservatives, stabilizers, wetting agents, emulsifiers, buffers etc.

Solid dosage forms for oral administration may include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound may be admixed with at least one inert diluent such as sucrose, lactose, or starch. Such dosage forms may also comprise, as in normal practice, additional substances other than inert diluents, e.g., lubricating agents such as magnesium stearate. In the case of capsules, tablets, and pills, the dosage forms may also comprise buffering agents. Tablets and pills can additionally be prepared with enteric coatings.

Liquid dosage forms for oral administration may include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs containing inert diluents commonly used in the art, such as water. Such compositions may also comprise adjuvants, such as wetting, sweetening, flavoring, and perfuming agents.

Compounds of the present invention can possess one or more asymmetric carbon atoms and are thus capable of existing in the form of optical isomers as well as in the form of racemic or non-racemic mixtures thereof. The optical isomers can be obtained by resolution of the racemic mixtures according to conventional processes, e.g., by formation of diastereoisomeric salts, by treatment with an optically active acid or base. Examples of appropriate acids are tartaric, diacetyltartaric, dibenzoyltartaric, ditoluoyltartaric, and camphorsulfonic acid and then separation of the mixture of diastereoisomers by crystallization followed by liberation of the optically active bases from these salts. A different process for separation of optical isomers involves the use of a chiral chromatography colurn optimally chosen to maximize the separation of the enantiomers. Still another available method involves synthesis of covalent diastereoisomeric molecules by reacting compounds of the invention with an optically pure acid in an activated form or an optically pure isocyanate. The synthesized diastereoisomers can be separated by conventional means such as chromatography, distillation, crystallization or sublimation, and then hydrolyzed to deliver the enantiomerically pure compound. The optically active compounds of the invention can likewise be obtained by using active starting materials. These isomers may be in the form of a free acid, a free base, an ester or a salt.

Likewise, the compounds of this invention may exist as isomers, that is compounds of the same molecular formula but in which the atoms, relative to one another, are arranged differently. In particular, the alkylene substituents of the compounds of this invention, are normally and preferably arranged and inserted into the molecules as indicated in the definitions for each of these groups, being read from left to right. However, in certain cases, one skilled in the art will appreciate that it is possible to prepare compounds of this invention in which these substituents are reversed in orientation relative to the other atoms in the molecule. That is, the substituent to be inserted may be the same as that noted above except that it is inserted into the molecule in the reverse orientation. One skilled in the art will appreciate that these isomeric forms of the compounds of this invention are to be construed as encompassed within the scope of the present invention.

The compounds of the present invention can be used in the form of salts derived from inorganic or organic acids. The salts include, but are not limited to, the following: acetate, adipate, alginate, citrate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, camphorate, camphorsulfonate, digluconate, cyclopentanepropionate, dodecylsulfate, ethanesulfonate, glucoheptanoate, glycerophosphate, hemisulfate, heptanoate, hexanoate, flumarate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, lactate, maleate, methansulfonate, nicotinate, 2-naphthalenesulfonate, oxalate, palmoate, pectinate, persulfate, 2-phenylpropionate, picrate, pivalate, propionate, succinate, tartrate, thiocyanate, tosylate, mesylate, and undecanoate. Also, the basic nitrogen-containing groups can be quaternized with such agents as lower alkyl halides, such as methyl, ethyl, propyl, and butyl chloride, bromides and iodides; dialkyl sulfates like dimethyl, diethyl, dibutyl, and diamyl sulfates, long chain halides such as decyl, lauryl, myristyl and stearyl chlorides, bromides and iodides, aralkyl halides like benzyl and phenethyl bromides, and others. Water or oil-soluble or dispersible products are thereby obtained.

Examples of acids that may be employed to from pharmaceutically acceptable acid addition salts include such inorganic acids as hydrochloric acid, sulfuric acid and phosphoric acid and such organic acids as oxalic acid, maleic acid, succinic acid and citric acid. Other examples include salts with alkali metals or alkaline earth metals, such as sodium, potassium, calcium or magnesium or with organic bases.

Also encompassed in the scope of the present invention are pharmaceutically acceptable esters of a carboxylic acid or hydroxyl containing group, including a metabolically labile ester or a prodrug form of a compound of this invention. A metabolically labile ester is one which may produce, for example, an increase in blood levels and prolong the efficacy of the corresponding non-esterified form of the compound. A prodrug form is one which is not in an active form of the molecule as administered but which becomes therapeutically active after some in vivo activity or biotransformation, such as metabolism, for example, enzymatic or hydrolytic cleavage. For a general discussion of prodrugs involving esters see Svensson and Tunek Drug Metabolism Reviews 165 (1988) and Bundgaard Design of Prodrugs, Elsevier (1985). Examples of a masked carboxylate anion include a variety of esters, such as alkyl (for example, methyl, ethyl), cycloalkyl (for example, cyclohexyl), aralkyl (for example, benzyl, p-methoxybenzyl), and alkylcarbonyloxyalkyl (for example, pivaloyloxymethyl). Amines have been masked as arylcarbonyloxymethyl substituted derivatives which are cleaved by esterases in vivo releasing the free drug and formaldehyde (Bungaard J. Med. Chem. 2503 (1989)). Also, drugs containing an acidic NH group, such as imidazole, imide, indole and the like, have been masked with N-acyloxymethyl groups (Bundgaard Design of Prodrugs, Elsevier (1985)). Hydroxy groups have been masked as esters and ethers. EP 039,051 (Sloan and Little, Apr. 11, 1981) discloses Mannich-base hydroxamic acid prodrugs, their preparation and use. Esters of a compound of this invention, may include, for example, the methyl, ethyl, propyl, and butyl esters, as well as other suitable esters formed between an acidic moiety and a hydroxyl containing moiety. Metabolically labile esters, may include, for example, methoxymethyl, ethoxymethyl, iso-propoxymethyl, α-methoxyethyl, groups such as α-((C₁-C₄)alkyloxy)ethyl, for example, methoxyethyl, ethoxyethyl, propoxyethyl, iso-propoxyethyl, etc.; 2-oxo-1,3-dioxolen-4-ylmethyl groups, such as 5-methyl-2-oxo-1,3,dioxolen-4-ylmethyl, etc.; C₁-C₃ alkylthiomethyl groups, for example, methylthiomethyl, ethylthiomethyl, isopropylthiomethyl, etc.; acyloxymethyl groups, for example, pivaloyloxymethyl, α-acetoxymethyl, etc.; ethoxycarbonyl-1-methyl; or α-acyloxy-α-substituted methyl groups, for example α-acetoxyethyl.

Further, the compounds of the invention may exist as crystalline solids which can be crystallized from common solvents such as ethanol, N,N-dimethylformamide, water, or the like. Thus, crystalline forms of the compounds of the invention may exist as polymorphs, solvates and/or hydrates of the parent compounds or their pharmaceutically acceptable salts. All of such forms likewise are to be construed as falling within the scope of the invention.

While the compounds of the invention can be administered as the sole active pharmaceutical agent, they can also be used in combination with one or more compounds of the invention or other agents. When administered as a combination, the therapeutic agents can be formulated as separate compositions that are given at the same time or different times, or the therapeutic agents can be given as a single composition.

The foregoing is merely illustrative of the invention and is not intended to limit the invention to the disclosed compounds. Variations and changes which are obvious to one skilled in the art are intended to be within the scope and nature of the invention which are defined in the appended claims.

From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions. 

1. A compound having the structure:

or any pharmaceutically-acceptable salt thereof, wherein: J is NH, O, S, S(═O) or S(═O)₂; X is N or C(R²); Y is N or C(R³); wherein no more than one of X and Y is N; n is independently, at each instance, 0, 1 or 2; R¹ is 4-tert-butylphenyl or 4-trifluoromethylphenyl substituted by 0, 1 or 2 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I; or R¹ is a pyridinyl or pyrimidinyl ring substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c); and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I; R² is selected from H, C₁₋₈alkyl, C₁₋₄haloalkyl, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), C(═O)NR^(a)R^(c), C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c); or R² is a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 1, 2 or 3 atoms selected from N, O and S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 0, 1, 2 or 3 groups selected from R^(f), halo, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c); or R² is C₁₋₄alkyl substituted by 0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c); R³ is (A) H; or (B) C₁₋₈alkyl substituted by 0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; or (C) a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 1, 2 or 3 atoms selected from N, O and S, wherein the ring is substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 0, 1, 2 or 3 groups selected from R^(f), halo, cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; or (D) —N(R^(a))—C₁₋₈alkyl, wherein the C₁₋₈alkyl is substituted by 0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; or (D) —OC₁₋₈alkyl, wherein the C₁₋₈alkyl is substituted by 0, 1, 2 or 3 groups selected from C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; or (E) halo, cyano, nitro, —C(═O)R^(f), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OC(═)R^(f), —OC(═O)OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g) and —N(R^(a))S(═O)₂NR^(a)R^(c), and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; R⁴ is phenyl, the phenyl being vicinally fused with a saturated, partially saturated or unsaturated 5- or 6-membered carbocyclic ring or a saturated, partially saturated or unsaturated 5- or 6-membered heterocyclic ring containing 1, 2 or 3 N atoms and 0 or 1 O or S atoms, wherein the phenyl and ring are substituted by 0, 1, 2 or 3 substituents independently selected from R^(c), oxo, R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(g), —C(═O)NR^(a)R^(g), —C(═NR^(a))NR^(a)R^(g), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c) and additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; provided R⁴ is not 6-(2H-benzo[b][1,4]oxazin-3(4H)-one) or any substituted version thereof; R⁵ is H or CH₃; R^(a) is independently, at each instance, H or R^(b); R^(b) is independently, at each instance, phenyl, benzyl or C₁₋₆alkyl, the phenyl, benzyl and C₁₋₆alkyl being substituted by 0, 1, 2 or 3 substituents selected from, C₁₋₄alkyl, C₁₋₃haloalkyl, —OC₁₋₄alkyl, —NH₂, —NHC₁₋₄alkyl and —N(C₁₋₄alkyl)C₁₋₄alkyl, and additionally substituted by 0, 1, 2, 3, 4, 5 or 6 substitutents independently selected from F, Cl, Br and I, R^(c) is independently at each instance a saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic ring containing 0, 1, 2, 3 or 4 atoms selected from N, O and S, wherein the carbon atoms of the ring are substituted by 0, 1 or 2 oxo or thioxo groups, sulfur atoms of the ring are substituted by 0, 1 or 2 oxo groups, nitrogen atoms of the ring are substituted by 0 or 1 oxo groups, and the ring is substituted by 0, 1, 2 or 3 substituents selected from C₁₋₈alkyl, C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(b), —C(═O)OR^(b), —C(═O)NR^(a)R^(a), —C(═NR^(a))NR^(a)R^(a), —OR^(a), —OC(═O)R^(b), —OC(═O)NR^(a)R^(a), —OC(═O)N(R^(a))S(═O)₂R^(b), —OC₂₋₆alkylNR^(a)R^(a), —OC₂₋₆alkylOR^(a), —SR^(a), —S(═O)R^(b), —S(═O)₂R^(b), —S(═O)₂NR^(a)R^(a), —S(═O)₂N(R^(a))C(═O)R^(b), —S(═O)₂N(R^(a))C(═O)OR^(b), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(a), —NR^(a)R^(a), —N(R^(a))C(═O)R^(b), —N(R^(a))C(═O)OR^(b), —N(R^(a))C(═O)NR^(a)R^(a), —N(R^(a))C(═NR^(a))NR^(a)R^(a), —N(R^(a))S(═O)₂R^(b), —N(R^(a))S(═O)₂NR^(a)R^(a), —NR^(a)C₂₋₆alkylNR^(a)R^(a) and —NR^(a)C₂₋₆alkylOR^(a), and the ring is additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; R^(d) is independently at each instance C₁₋₈alkyl, C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(b), —C(═O)OR^(b), —C(═O)NR^(a)R^(a), —C(═NR^(a))NR^(a)R^(a), —OR^(a), —OC(═O)R^(b), —OC(═O)NR^(a)R^(a), —OC(═O)N(R^(a))S(═O)₂R^(b), —OC₂₋₆alkylNR^(a)R^(a), —OC₂₋₆alkylOR^(a), —SR^(a), —S(═O)R^(b), —S(═O)₂R^(b), —S(═O)₂NR^(a)R^(a), —S(═O)₂N(R^(a))C(═O)R^(b), —S(═O)₂N(R^(a))C(═O)OR^(b), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(a), —NR^(a)R^(a), —N(R^(a))C(═O)R^(b), —N(R^(a))C(═O)OR^(b), —N(R^(a))C(═O)NR^(a)R^(a), —N(R^(a))C(═NR^(a))NR^(a)R^(a), —N(R^(a))S(═O)₂R^(b), —N(R^(a))S(═O)₂NR^(a)R^(a), —NR^(a)C₂₋₆alkylNR^(a)R^(a) or —NR^(a)C₂₋₆alkylOR^(a); R^(e) is independently at each instance R^(d) or H; R^(f) is independently at each instance C₁₋₈alkyl substituted by 0, 1, 2 or 3 substituents independently selected from C₁₋₄haloalkyl, cyano, nitro, —C(═O)R^(b), —C(═O)OR^(b), C(═O)NR^(a)R^(a), —C(═NR^(a))NR^(a)R^(a), —OR^(a), —OC(═O)R^(b), —OC(═O)NR^(a)R^(a), —OC(═O)N(R^(a))S(═O)₂R^(b), —OC₂₋₆alkylNR^(a)R^(a), —OC₂₋₆alkylOR^(a), —SR^(a), —S(═O)R^(b), —S(═O)₂R^(b), —S(═O)₂NR^(a)R^(a), —S(═O)₂N(R^(a))C(═O)R^(b), —S(═O)₂N(R^(a))C(═O)OR^(b), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(a), —NR^(a)R^(a), —N(R^(a))C(═O)R^(b), —N(R^(a))C(═O)OR^(b), —N(R^(a))C(═O)NR^(a)R^(a), —N(R^(a))C(═NR^(a))NR^(a)R^(a), —N(R^(a))S(═O)₂R^(b), —N(R^(a))S(═O)₂NR^(a)R^(a), —NR^(a)C₂₋₆alkylNR^(a)R^(a) and —NR^(a)C₂₋₆alkylOR^(a); and additionally substituted by 0 or 1 saturated, partially saturated or unsaturated 5-, 6- or 7-membered monocyclic or 6-, 7-, 8-, 9-, 10- or 11-membered bicyclic rings containing 0, 1, 2, 3 or 4 atoms selected from N, O and S, wherein the carbon atoms of the ring are substituted by 0, 1 or 2 oxo or thioxo groups, sulfur atoms of the ring are substituted by 0, 1 or 2 oxo groups, nitrogen atoms of the ring are substituted by 0 or 1 oxo groups, and the ring is substituted by 0, 1, 2 or 3 substituents selected from C₁₋₈alkyl, C₁₋₄haloalkyl, halo, cyano, nitro, —C(═O)R^(b), —C(═O)OR^(b), —C(═O)NR^(a)R^(a), —C(═NR^(a))NR^(a)R^(a), —OR^(a), —C(═O)R^(b), —C(═O)NR^(a)R^(a), —OC(═O)N(R^(a))S(═O)₂R^(b), —OC₂₋₆alkylNR^(a)R^(a), —OC₂₋₆alkylOR^(a), —SR^(a), —S(═O)R^(b), —S(═O)₂R^(b), —S(═O)₂NR^(a)R^(a), —S(═O)₂N(R^(a))C(═O)R^(b), —S(═O)₂N(R^(a))C(═O)OR^(b), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(a), —NR^(a)R^(a), —N(R^(a))C(═O)R^(b), —N(R^(a))C(═O)OR^(b), —N(R^(a))C(═O)NR^(a)R^(a), —N(R^(a))C(═NR^(a))NR^(a)R^(a), —N(R^(a))S(═O)₂R^(b), —N(R^(a))S(═O)₂NR^(a)R^(a), —NR^(a)C₂₋₆alkylNR^(a)R^(a) and —NR^(a)C₂₋₆alkylOR^(a); and the C₁₋₈alkyl and ring are additionally substituted by 0, 1, 2, 3, 4 or 5 substituents independently selected from Br, Cl, F and I; and R^(g) is independently at each instance R^(e) or H.
 2. A compound according to claim 1 selected from the group of: 6-(1H-indol-5-yl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; 6-(2,3-dihydro-1,4-benzodioxin-6-yl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; 6-(2,3-dihydro-1-benzofuran-5-yl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; 6-(3,4-dihydro-2H-1,5-benzodioxepin-7-yl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; 6-(5-isoquinolinyl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; 6-(5-quinolinyl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; 6-(6-quinolinyl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; 6-(6-quinoxalinyl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; 6-(7-quinolinyl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; 6-(8-quinolinyl)-N-(4-(trifluoromethyl)phenyl)-4-pyrimidinamine; and 7-(6-((4-(trifluoromethyl)phenyl)oxy)-4-pyrimidinyl)quinoline; or any pharmaceutically-acceptable salt thereof.
 3. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically-acceptable diluent or carrier.
 4. A compound according to claim 1, wherein R¹ is 4-tert-butylphenyl or 4—trifluoromethylphenyl substituted by 0, 1 or 2 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I.
 5. A compound according to claim 1, wherein R¹ is a pyridinyl or pyrimidinyl ring substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I.
 6. A compound according to claim 1, wherein: X is N; Y is CH; R¹ is 4-tert-butylphenyl or 4-trifluoromethylphenyl substituted by 0, 1 or 2 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(r), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I; and R⁵ is H.
 7. A compound according to claim 1, wherein: X is CH; Y is CH; R¹ is 4-tert-butylphenyl or 4-trifluoromethylphenyl substituted by 0, 1 or 2 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)OR^(g), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)R^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)R^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I; and R⁵ is H.
 8. A compound according to claim 1, wherein: X is N; Y is CH; R¹ is a pyridinyl or pyrimidinyl ring substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)F^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I; and R⁵ is H.
 9. A compound according to claim 1, wherein: X is CH; Y is CH; R¹ is a pyridinyl or pyrimidinyl ring substituted by 1, 2 or 3 groups selected from R^(f), cyano, nitro, —C(═O)R^(f), —C(═O)OR^(f), —C(═O)NR^(a)R^(f), —C(═NR^(a))NR^(a)R^(f), —OR^(g), —OC(═O)R^(f), —OC(═O)NR^(a)R^(g), —OC(═O)N(R^(a))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(g), —OC₂₋₆alkylOR^(g), —SR^(f), —S(═O)R^(f), —S(═O)₂R^(f), —S(═O)₂NR^(a)R^(f), —S(═O)₂N(R^(a))C(═O)R^(f), —S(═O)₂(R^(a))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(g), —NR^(a)R^(g), —N(R^(a))C(═O)R^(f), —N(R^(a))C(═O)NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(g), —N(R^(a))S(═O)₂R^(f), —N(R^(a))S(═O)₂NR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylOR^(g), —C(═O)R^(c), —C(═O)OR^(c), —C(═O)NR^(a)R^(c), —C(═NR^(a))NR^(a)R^(c), —OR^(c), —OC(═O)R^(c), —OC(═O)NR^(a)R^(c), —OC(═O)N(R^(a))S(═O)₂R^(c), —OC(═O)N(R^(c))S(═O)₂R^(f), —OC₂₋₆alkylNR^(a)R^(c), —OC₂₋₆alkylOR^(c), —SR^(c), —S(═O)R^(c), —S(═O)₂R^(c), —S(═O)₂NR^(a)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(f), —S(═O)₂N(R^(a))C(═O)R^(c), —S(═O)₂N(R^(c))C(═O)OR^(g), —S(═O)₂N(R^(a))C(═O)OR^(c), —S(═O)₂N(R^(c))C(═O)NR^(a)R^(g), —S(═O)₂N(R^(a))C(═O)NR^(a)R^(c), —NR^(a)R^(c), —N(R^(c))C(═O)F^(f), —N(R^(a))C(═O)R^(c), —N(R^(c))C(═O)OR^(g), —N(R^(a))C(═O)OR^(c), —N(R^(c))C(═O)NR^(a)R^(g), —N(R^(a))C(═O)NR^(a)R^(c), —N(R^(c))C(═NR^(a))NR^(a)R^(g), —N(R^(a))C(═NR^(a))NR^(a)R^(c), —N(R^(c))S(═O)₂R^(f), —N(R^(a))S(═O)₂R^(c), —N(R^(c))S(═O)₂NR^(a)R^(g), —N(R^(a))S(═O)₂NR^(a)R^(c), —NR^(c)C₂₋₆alkylNR^(a)R^(g), —NR^(a)C₂₋₆alkylNR^(a)R^(c), —NR^(c)C₂₋₆alkylOR^(g) and —NR^(a)C₂₋₆alkylOR^(c), and additionally substituted by 0, 1, 2, 3 or 4 substituents independently selected from Br, Cl, F and I; and R⁵ is H. 